The aim of the present work was to investigate the initial stages of NH3 in
teraction with nickel oxide layers formed on well-defined Ni(111) surfaces,
The selected technique was x-ray photoelectron spectroscopy, Ammonia adsor
ption was performed at 10(-7) mbar and room temperature in a preparation ch
amber attached to the analysis chamber. After each adsorption, the N Is cor
e level was analysed and its intensity was plotted as a function of exposur
e (at the same pressure) to obtain the adsorption kinetics. The XPS peak sh
apes and the chemical shifts were related to the nature of the adsorption p
roducts, In our experimental renditions, we observed that the more reactive
initial surface was the one covered by the O-adsorbed phase corresponding
to the precursor state of the NiO formation. The NiO alone does not exhibit
significant reactivity, whereas a mixture of NiO and the O-adsorbed phase
shows a similar behaviour to that of the pure O-adsorbed phase. From the fi
rst adsorption until the last one, two nitrogen adspecies were detected: on
e with an N 1s binding energy (BE) of 397.8 eV and the other at 399.7 eV, T
he data indicate that the surface reactivity is structure-sensitive for the
NiO layer and the mechanisms of adsorption seem to involve NH3 dissociatio
n into NHx adspecies, along with OH formation. Copyright (C) 2000 John Whey
& Sons, Ltd.